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U. S. Department of Agriculture,2 ,3,, Beltsville, MD 20705
Abstract
Pale, soft and exudative pork (PSE) is associated with a rapid rate of postmortem glycogenolysis of muscle, accumulation of lactic acid and a concomitant decline of pH. This study was designed to examine the effects of chronic Prednisolone (CP), acute Prednisolone (AP) or chronic epinephrine (CE) treatment on epinephrine-induced PSE development. All pigs were fed 25% sucrose for 10 days prior to slaughter, and each pig received a 5 mg intravenous injection of epinephrine 5 min prior to slaughter. All three treated groups of swine had higher (P<.05) 3-min postmortem muscle glycogen values (CP-65.8, AP-59.4, and CE-67.2 µMoles glucosyl units/g) than the controls (43.7 µMoles glucosyl units/gram). Phosphorylase activities did not differ between treated and control swine, but tended to be lower in the CE swine. Muscle lactate values at 3 min did not differ between treated and control swine. Lactate values exceeded published values, however, and indicated that antemortem stress (epinephrine injection) influenced postmortem glycolytic rate as early as 3 min after exsanguination. Visual inspection and percentage reflectance at 24 hr postmortem indicated that 6 of 6 CP, 4 of 5 AP, 2 of 5 CE and 10 of 10 controls developed PSE musculature. These data indicate that antemortem treatment with Prednisolone (either chronic or acute) does not prevent the formation of epinephrine-induced PSE muscle. The CE treatment reduced the incidence of PSE, possibly due to an auto feedback mechanism that caused a reduction in muscle epinephrine receptors resulting from the chronically elevated epinephrine.
1 Department of Animal Science, Mississippi State University, Starkville 39762; formerly with the Meat Science Research Laboratory, FR, USDA
2 Nonruminant Nutrition Laboratory.
3 Meat Science Research Laboratory.
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